Botensilimab plus balstilimab in relapsed/refractory microsatellite stable metastatic colorectal cancer: a phase 1 trial

Microsatellite stable metastatic colorectal cancer (MSS mCRC; mismatch repair proficient) has previously responded poorly to immune checkpoint blockade. Botensilimab (BOT) is an Fc-enhanced multifunctional anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antibody designed to expand therapy to cold/poorly immunogenic solid tumors, such as MSS mCRC. BOT with or without balstilimab (BAL; anti-PD-1 antibody) is being evaluated in an ongoing expanded phase 1 study. The primary endpoint is safety and tolerability, which was evaluated separately in the dose-escalation portion of the study and in patients with MSS mCRC (using combined dose-escalation/dose-expansion data). Secondary endpoints include investigator-assessed RECIST version 1.1–confirmed objective response rate (ORR), disease control rate (DCR), duration of response (DOR) and progression-free survival (PFS). Here we present outcomes in 148 heavily pre-treated patients with MSS mCRC (six from the dose-escalation cohort; 142 from the dose-expansion cohort) treated with BOT and BAL, 101 of whom were considered response evaluable with at least 6 months of follow-up. Treatment-related adverse events (TRAEs) occurred in 89% of patients with MSS mCRC (131/148), most commonly fatigue (35%, 52/148), diarrhea (32%, 47/148) and pyrexia (24%, 36/148), with no grade 5 TRAEs reported and a 12% discontinuation rate due to a TRAE (18/148; data fully mature). In the response-evaluable population (n = 101), ORR was 17% (17/101; 95% confidence interval (CI), 10–26%), and DCR was 61% (62/101; 95% CI, 51–71%). Median DOR was not reached (NR; 95% CI, 5.7 months–NR), and median PFS was 3.5 months (95% CI, 2.7–4.1 months), at a median follow-up of 10.3 months (range, 0.5–42.6 months; data continuing to mature). The combination of BOT plus BAL demonstrated a manageable safety profile with no new immune-mediated safety signals and encouraging clinical activity with durable responses. ClinicalTrials.gov identifier: NCT03860272.


Article
https://doi.org/10.1038/s41591-024-03083-7 in tumors classified as 'cold' or refractory to prior ICB.In addition to complete blockade of CTLA-4 ligand interactions, the Fc-enhanced IgG1 region of BOT binds with increased binding affinity to activating FcγRs on APCs and NK cells, including both FcγRIIIA variants, low-affinity F158 and high-affinity V158, compared to conventional IgG1 anti-CTLA-4 antibodies (for example, ipilimumab).Therefore, in addition to blocking CTLA-4, BOT promotes optimized T cell priming, activation and memory formation by strengthening APC and T cell co-engagement 23 .As an Fc-enhanced anti-CTLA-4 antibody, BOT also promotes intratumoral T reg depletion via antibody-dependent cellular cytotoxicity and phagocytosis mechanisms.These qualities differentiate BOT from approved CTLA-4 antibodies with the potential for BOT to extend benefit to 'cold' or ICB-refractory tumors by activating both the innate and adaptive immune system 25,26 .Balstilimab (AGEN2034; BAL) is a fully human monoclonal antibody that binds with high affinity to PD-1, preventing the interaction between the receptor and its ligands PD-L1 and/or PD-L2 with a similar efficacy and safety profile to currently approved PD-1 inhibitors 27 .
A phase 1, open-label study of BOT with or without BAL was initiated in multiple relapsed/refractory (R/R) solid tumors (NCT03860272) to assess safety and tolerability as well as to test if the specific design of BOT translates into clinical benefit.The study began with the dose escalation of BOT monotherapy and then the BOT and BAL combination, followed by disease-specific expansion cohorts, including one that enrolled patients with MSS mCRC for treatment with BOT monotherapy or combination therapy.Here we report safety and preliminary efficacy outcomes for the heavily pre-treated MSS mCRC patient population treated in this phase 1 study.

Dose escalation
The dose-escalation portion of the C-800-01 study (3 + 3 design) occurred from 1 April 2019 to 31 August 2023 (data cutoff: 29 November 2023), whereby 83 patients with advanced solid tumors (including 10 patients with MSS mCRC) were enrolled and treated with BOT monotherapy every 3 weeks (Q3W) or 6 weeks (Q6W; staggered with Q3W dosing), starting at dose level 0.1 mg kg −1 up to 3 mg kg −1 , administered intravenously (IV) for up to 2 years, or in combination with BAL 3 mg kg −1 every 2 weeks (Q2W), administered IV for up to 2 years.Patients could be treated beyond progression.A total of 48 patients were treated with BOT monotherapy, and 35 patients received the combination of BOT plus BAL (Fig. 1 and Extended Data Fig. 1).Baseline demographics and disease characteristics for all dose-escalation cohorts are summarized in Extended Data Table 1.
There were no dose-limiting toxicities (DLTs) in either BOT monotherapy or BOT plus BAL combination therapy dose-escalation cohorts, which was the primary endpoint of the study.A maximum tolerated dose was not reached, and further investigation is warranted to determine the recommended phase 2 dose (RP2D) by disease indication.Both monotherapy and combination therapy dose-escalation cohorts received a median of two BOT doses (range, 1-23 BOT monotherapy; range, 1-17 combination therapy; Supplementary Tables 1 and 2).A secondary endpoint was assessing the severity and causality of treatment-emergent adverse events (TEAEs) for all dose groups.Treatment-related adverse events (TRAEs) of any grade, defined as TEAEs related to BOT or BAL, occurred in 75% of monotherapy patients (36/48; 33% grade ≥3) and in 83% of combination therapy patients (29/35; 26% grade ≥3).Additional safety data from the dose-escalation portion of the study are summarized in Supplementary Tables 3 and 4.
Other secondary endpoints include objective response rate (ORR), disease control rate (DCR, defined as a best response of complete response (CR), partial response (PR) or stable disease (SD) for at least 6 weeks) and progression-free survival (PFS) for all dose groups per Response Evaluation Criteria in Solid Tumors version 1.1 Colorectal cancer (CRC) is the second leading cause of cancer death in the United States, comprising an estimated 8.3% of cancer-related deaths annually 1 .Although overall mortality from CRC has declined, survival remains poor for advanced disease, and the burden is shifting to a younger population 2 .Alarmingly, from 1995 to 2019, the number of patients under the age of 55 who were diagnosed with CRC in the United States nearly doubled 3 .
Chemotherapy remains the cornerstone of treatment, and although survival has increased with the addition of monoclonal antibodies targeting vascular endothelial growth factor (VEGF) and epidermal growth factor receptors (EGFRs), improvements have been moderate [4][5][6][7][8] .Immunotherapy using checkpoint inhibitors targeting programmed cell death (ligand) 1 (PD-(L)1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) have become established pillars of systemic therapy across oncology, often achieving durable remissions.However, response rates vary across tumor types, with particularly disappointing outcomes in patients with metastatic colorectal cancer (mCRC) that is not microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) and is commonly referred to as microsatellite stable (MSS) or mismatch repair proficient [9][10][11][12] .Since their initial approval in metastatic melanoma 13 , immune checkpoint blockade (ICB) regimens have demonstrated efficacy but only gained regulatory approval in select gastrointestinal cancers, such as gastroesophageal cancer and, more recently, cholangiocarcinoma 14,15 .
The only patients with mCRC for whom ICB has been shown to be efficacious and is approved are the approximately 4% with MSI-H or dMMR tumors, in whom response rates are around 40% and higher, likely due to increased neoantigen load [16][17][18] .Conversely, response rates to PD-(L)1 inhibition in MSS mCRC are near 0%, and immunotherapy-only combinations including PD-(L)1/CTLA-4 have also demonstrated limited efficacy 19 .The combination of durvalumab (anti-PD-1 antibody) and tremelimumab (anti-CTLA-4 antibody) was evaluated in a randomized phase 2 study in patients with mCRC and resulted in one objective response out of 119 patients, a median progression-free survival (PFS) of 1.8 months and a median overall survival (OS) of 6.6 months.Similarly, nivolumab (anti-PD-1 antibody) and ipilimumab (anti-CTLA-4 antibody) were evaluated in two separate trials with disappointing efficacy: the TAPUR phase 2 basket study examined individuals in whom all lines of therapy had been exhausted and reported results from patients with mCRC with high tumor mutational burden (TMB; defined as ≥9 mutations per megabase (Mut/Mb)) treated with nivolumab and ipilimumab 20 .There was only one response out of 10 patients treated, a median PFS of 3.1 months and a median OS of 9.9 months.Similarly, in the CheckMate-142 study, only one of 23 patients with MSS mCRC treated with ipilimumab and nivolumab responded 16 .
MSS mCRC can be classified as poorly immunogenic or 'cold', with a tumor microenvironment (TME) commonly infiltrated by immunosuppressive regulatory T cells (T regs ) and myeloid cells and characteristically absent of CD8 + effector T cells (T effectors ) 17 .A multitude of tumor-intrinsic and tumor-extrinsic factors, such as low TMB and dysfunctional adaptive immunity, for example, may contribute to refractoriness to ICB and resistance to other primary and adaptive immunotherapies in MSS mCRC 17,18,21,22 .
Fragment crystallizable gamma receptor (FcγR) interactions have been shown to play a central role in antibody-directed immune effector cell activities.For anti-CTLA-4 antibodies, the interaction with FcγR on antigen-presenting cells (APCs) and natural killer (NK) cells enhances antigen-specific T cell responses and tumoricidal activity 23 .Furthermore, human FcγRIIIA polymorphisms, along with neoantigen burden, have been shown to impact responses to ipilimumab in patients with advanced melanoma 24 .
Botensilimab (AGEN1181; BOT) is a novel multifunctional Fc-enhanced anti-CTLA-4 antibody intentionally designed to overcome the limitations of conventional ICB and address the unmet need Article https://doi.org/10.1038/s41591-024-03083-7(RECIST 1.1), based on investigator assessment, as well as pharmacokinetics and immunogenicity.Imaging was performed Q6W (±3 d).Objective responses were observed in eight of 83 dose-escalation patients (10%; 95% confidence interval (CI), 4-18%).Among monotherapy patients, a patient with PD-1 R/R endometrial carcinoma achieved a CR, and a patient with PD-1 R/R cervical cancer achieved a PR.In the combination dose-escalation cohorts, six patients achieved a PR-three with MSS mCRC, two with platinum resistant/refractory ovarian cancer and one with endometrial carcinoma.An additional 28 patients (34%) had SD, and the DCR was 43% (95% CI, 33-55%) as of the data cutoff (29 November 2023).Median follow-up was 6.3 months (range, 0.7-42.6months), and the median duration of response (DOR) was not reached (NR; 95% CI, 4.2 months-NR).Additional efficacy analyses in all dose-escalation cohorts are provided in Extended Data Table 2.As part of a protocol amendment, patients were permitted to cross over from BOT monotherapy to the combination upon progression.Out of 13 total patients who first received BOT monotherapy and later crossed over to the combination, there were four responders (two patients with MSS mCRC, one with dedifferentiated liposarcoma and one with platinum resistant/refractory ovarian cancer).

Article
https://doi.org/10.1038/s41591-024-03083-7 In a separate pharmacokinetic and immunogenicity analysis, BOT exhibited dose-proportional increases in exposure metrics (maximum concentration (C max ), minimum concentration (C min ) and trough concentration (C trough )) across the dose range of 0.1 mg kg −1 to 3 mg kg −1 for monotherapy and 0.1 mg kg −1 to 2 mg kg −1 in combination with BAL.After administration of a single dose of BOT at 1 mg kg −1 Q6W, geometric mean C max was 22.64 μg ml −1 for monotherapy and 19.08 μg ml −1 in combination with BAL.At steady state, geometric mean C max was 23.86 μg ml −1 for monotherapy and 20.12 μg ml −1 in combination with BAL at the same dose level.The estimated geometric mean terminal half-life of BOT was approximately 14 d.In addition, in a small number of patients who were positive for antidrug antibodies (ADAs), the potential impact on BOT pharmacokinetics was assessed.Exposure levels were similar between patients who were ADA positive or negative.

MSS mCRC patient characteristics
Patients were subsequently enrolled in select disease-specific expansion cohorts as the dose escalation was completed, including MSS mCRC, sarcomas, ovarian cancer, PD-1 R/R melanoma, PD-1 R/R hepatocellular carcinoma, PD-1 R/R non-small cell lung cancer and others (Fig. 1 and Extended Data Fig. 1).As of the data cutoff (29 November 2023), a total of 148 patients with MSS mCRC were treated with BOT 1 mg kg −1 or 2 mg kg −1 Q6W plus BAL 3 mg kg −1 Q2W (with prior ICB permitted).Of note, 10 patients with MSS mCRC were included in the dose-escalation portion of the study-four who received BOT monotherapy (0.3 mg kg −1 Q3W, 1 mg kg −1 Q3W, 1 mg kg −1 Q6W and 2 mg kg −1 Q6W) and six who received the BOT and BAL combination (two who received 1 mg kg −1 BOT and four who received 2 mg kg −1 BOT); and 142 patients were from the MSS mCRC expansion cohort (an additional patient was enrolled but never received treatment).In this population, approximately 79% of responses to BOT and BAL are observed by 6 months (excluding patients who left the study early).Based on these response kinetics, 101 with at least 6 months of follow-up out of the total 148 patients with MSS mCRC treated with 1 mg kg −1 or 2 mg kg −1 of BOT and BAL were considered response evaluable (Fig. 1).
Baseline demographics and disease characteristics are summarized in Table 1 for all treated patients (and broken down by response-evaluable patients (n = 101) and additional treated patients (n = 47) in Extended Data Table 3).Median age was 56 years (range, 25-82).Seventy-six patients (51%) were female, and 79 (53%) had an Eastern Cooperative Oncology Group (ECOG) performance status of 1.This patient population was heavily pre-treated with a median of three prior lines of therapy (range, 1-10), and 24 of 148 patients (16%) had received prior PD-(L)1 inhibitors (three of whom also received prior CTLA-4 inhibition when prior protocol versions allowed).There were 25 patients (17%) with active liver metastases (LM) and 123 patients (83%) with no active liver metastases (NLM).Patients with NLM were further broken down into patients with treated LM (20 patients (14%)), defined as having LM that were resected, ablated or treated with stereotactic body radiation therapy without recurrence and patients with no history of LM (103 patients (70%)).One hundred patients (68%) had more than one site of metastatic disease, and 42% had peritoneal disease.Of 40 patients in whom TMB data from central assessment were readily available, only one had a TMB > 10 Mut/Mb (TMB = 13 Mut/Mb; via whole-exome sequencing (WES); Personalis ImmunoID NeXT assay).Of the 45 patients in whom mutation data were available, 26 (58%) harbored RAS mutations, and two (4%) had BRAF mutations (as detected with the Personalis ImmunoID NeXT assay).
Grade 3 TRAEs occurred in 31% of patients (46/148) and included eight cases (5%) of diarrhea; six cases of immune-mediated enterocolitis (4%); four cases each (3%) of colitis and pyrexia; three cases of acute Based on data supporting the use of tumor necrosis factor (TNF) inhibitors in the steroid-sensitive setting and clinical practice, infliximab was used to manage the immune-mediated TRAE of diarrhea/ colitis in this study even in the non-refractory low-grade setting 28,29 .Patients who received infliximab were able to continue on study drug if toxicity resolved and was not higher than grade 2. If a patient had a grade 3 event related to BOT but not to BAL, they were allowed to continue BAL.Of 36 total patients who received immunosuppressants for an immune-mediated TRAE of diarrhea/colitis, 35 received infliximab (97%), and 31 received concurrent steroids (86%).Nineteen of these 36 patients (30 events; four grade 1 events, 13 grade 2 events, two grade 3 events) either temporarily stopped BOT or remained on treatment.Thirty-one of those 36 patients had complete resolution of diarrhea/colitis, and five patients had unresolved diarrhea/colitis (two with sequelae), suggesting that early treatment with infliximab can effectively manage immune-mediated treatment-related diarrhea/ colitis 29 .Other TRAEs were managed according to guidelines at the investigator's discretion 30 .

Efficacy
Of the 148 treated patients with MSS mCRC, 101 with at least 6 months of follow-up were evaluated in efficacy analyses (including four patients from the dose-escalation portion of the study and 97 from the dose-expansion portion; data on the additional 47 treated patients are continuing to mature).Objective responses were observed in 17 of 101 patients (17%; 95% CI, 10-26%), including one CR (Fig. 2a).An additional 45 patients (45%) had SD, and the DCR was 61% (95% CI, 51-71%; Fig. 2b).The clinical benefit rate (CBR, defined as best response of CR, PR or SD for at least 24 weeks) was 28% (95% CI, 19-38%).The median DOR was NR (95% CI, 5.7 months-NR), and the median PFS was 3.5 months (95% CI, 2.7-4.1 months) (Fig. 3a).A final exploratory endpoint assessed median OS and/or rate of OS.The median OS was 20.9 months (95% CI, 10.6 months-NR) (Fig. 3b), and the 12-month OS rate was 60% (95% CI, 49-69%), with a median follow-up of 10.3 months (range, 0.5-42.6months).Eleven of the 17 responding patients had ongoing responses at the time of the data cutoff.An additional PR was confirmed after the data cutoff (18/101; ORR 18%).Five patients had at Hyperhidrosis 10 ( 7) Blood alkaline phosphatase increased 6 least 30% reduction in target lesions, as noted in Fig. 2a, although these responses did not qualify as RECIST-confirmed responses.One patient later had progressive disease (PD); one received surgery at 20 weeks and was unevaluable; one initially had a response until 60 weeks that was changed to a best response of SD after a small peri-splenic nodule at week 66 was observed that was retrospectively identified as being present since week 18 (with all other lesions remaining in a response); one had a RECIST response at 6 weeks and had a surgical resection of a target lesion that was considered clinical progression based on increase from nadir at 12 weeks (after receiving steroids for an immune-mediated TRAE) and was not confirmed, the remaining target lesions then progressed; and another patient had a PR in target lesions but experienced recurrence of treated LM at week 18.In the additional 47 treated patients with fewer than 6 months of follow-up, several objective responses have been observed thus far, although the median follow-up for these patients is only 3.3 months (range, 1.9-4.9months).Updates will be provided as the data reach maturity.

Analysis by liver involvement
An exploratory analysis by liver involvement was conducted early in the study, and more favorable outcomes were observed in patients with NLM (Figs. 2a,b and 3a,b).The protocol was subsequently amended to focus on patients with NLM to reduce heterogeneity and complexity in the phase 1 patient population.

Biomarker and gene expression analysis
Exploratory endpoints in this study included investigating biomarkers that may predict pharmacologic activity or response to BOT with or without BAL and exploring immune biomarkers in peripheral blood and tumor tissue.Thus, pre-treatment tumor tissue was analyzed to characterize potential genomic and biomarker differences among responders, patients with SD (of at least 12 weeks) and those with PD (per RECIST 1.1).Local and central genomics testing with the Personalis ImmunoID NeXT assay was available for nine of the 17 responders.Only one had a TMB ≥ 10 Mut/Mb at 13 Mut/Mb; four had RAS mutations (KRAS G12D , KRAS G13D , NRAS Q61R and KRAS Q61L ); and one had a BRAF G466V mutation.
In patients with available TMB data (n = 38), no significant differences were observed among responders, patients with SD or those with PD (Supplementary Fig. 1).Regarding PD-L1 expression, there are significant limitations of this dataset, making interpretation inconclusive at this time.Limitations include that PD-L1 expression was not available/assessed in all patients; biopsies were not tested consistently across sites; samples were of varying age with varying intervening treatments; and some sites were tested for PD-L1 as part of a local testing panel, whereas a subset of available samples was tested as part of the trial exploratory endpoints through a non-clinically validated, research-based PD-L1 test, 28-8, which was conducted centrally.Furthermore, there was some level of discordance between local and central testing, and the data were confounded by multiple variables.We provided response characteristics of individual responders in Fig. 4 and non-responders in Extended Data Fig. 2 and biomarker and genomics data by individual patient in Supplementary Table 7, but we have not analyzed these data due to the abovementioned limitations.
To determine differences in specific immune cell signatures at the RNA level at baseline (pre-treatment), RNA sequencing (RNA-seq) on bulk tumor tissue was performed, followed by determining normalized gene transcript per million counts.Counts were transformed into z-score values whereby gene signatures were summarized by averaging the gene expression values by sample using previously published gene signatures associated with response to ICB 31,32 .Based on low numbers of patients with available tissue for RNA-seq (nine responders; 18 with SD (≥12 weeks); and 11 with PD), statistically significant patterns were not identified among responders, those with SD or those with PD (Extended Data Fig. 3 and Supplementary Table 8) 32 .

Discussion
MSS mCRC remains a significant clinical challenge, especially for patients who have progressed after standard chemotherapy and anti-VEGF or anti-EGFR antibodies.Available therapies have limited efficacy, and outcomes are generally poor [33][34][35] .To date, ICB has been ineffective in this patient population.Based on data that Fc-enhanced CTLA-4 inhibitors may overcome some mechanisms of resistance to ICB in immunologically 'cold' tumors, we investigated the safety and efficacy of BOT, a multifunctional Fc-enhanced CTLA-4 inhibitor, in combination with BAL, a PD-1 inhibitor, in patients with heavily pre-treated MSS mCRC.Non-clinical studies suggest that anti-CTLA-4 antibodies engineered with enhanced binding to activating FcγRs on APCs improve T cell priming and activation, along with greater T reg depletion via engagement of NK cells 23,24,36 .These mechanisms may overcome the immunosuppressive TME of mCRC and drive responses even in patients with MSS and/or low TMB tumors.In this phase 1 study including 83 patients from the dose-escalation portion of the study and 148 patients with R/R MSS mCRC treated with the combination of BOT and BAL, we showed a manageable safety profile and encouraging efficacy across tumor types.This is the first time, to our knowledge, that consistent and durable responses to ICB have been reported in difficult-to-treat patients with MSS mCRC.The safety profile of the BOT and BAL combination appears manageable and distinct from approved ICB.This is consistent with BOT's design, which reduces complement fixation, thereby avoiding irreversible complement-mediated toxicity, such as hypophysitis 37 .Rates of high-grade treatment-related visceral toxicities outside of the gastrointestinal tract, such as hypophysitis, myocarditis, pneumonitis and hepatitis, were rare and compare favorably with other ICB combinations [38][39][40][41] .Notably, among the 148 patients with refractory CRC treated, diarrhea was the main clinically significant TRAE in 32% of patients.Based on emerging data that TNF inhibitors may allow effective management of ICB-related diarrhea/colitis, the study protocol recommended treatment with infliximab even for first-line treatment for a low-grade immune-mediated TRAE of diarrhea/colitis.Emerging evidence from clinical trials investigating CTLA-4 inhibition in lung cancer and other malignancies suggests that discontinuing therapy due to a TRAE or requiring immunosuppression to manage immune-mediated toxicities does not impact OS negatively [42][43][44] .Most notably, the combination of BOT and BAL resulted in promising efficacy, with an ORR of 17% (17/101 patients; ORR 18% with an additional response that was confirmed after the data cutoff) and a DCR of 61% (62/101) in patients with heavily pre-treated and refractory MSS mCRC (Figs. 2 and 3).
Patients without LM comprise approximately one-third of the mCRC population and have a better prognosis, although even these patients have limited clinical benefit with approved therapies [45][46][47][48] .The Aide et Recherche en Cancérologie Digestive Metastatic Colorectal Cancer Database comprises approximately 50 global randomized clinical trials and included about 40,000 patients with mCRC, including data from the CORRECT and RECOURSE phase 3 studies that evaluated regorafenib and trifluridine/tipiracil, respectively.In patients who received placebo, median OS in NLM patients versus those with LM was 7.9 months versus 4.1 months, and the ORR was 1.3% versus 0%.The NLM subgroup had modestly superior benefits from treatment versus the LM group (OS hazard ratio of treatment versus placebo was 0.60 versus 0.67, respectively); median OS and ORR in patients with NLM treated with trifluridine/tipiracil or regorafenib was 12.9 months (95% CI, 11.9-17.3)and 2.8% (95% CI, 1.3-5.6),respectively 49 .
As observed with other ICB agents, the presence or absence of LM may also impact the efficacy of BOT and BAL 50,51 .We prospectively enrolled patients with and without active LM to address this question and later enriched for patients with NLM with a protocol amendment.In our study, all objective responses were observed in patients with NLM (Figs. 2 and 3).There was a period during the study when, based  on an amendment, only patients with no history of LM were enrolled; subsequently, enrollment was reopened to patients with treated LM as in the ongoing phase 2 study with a US Food and Drug Administration fast-track designation.Within the limitations of this smaller population of 16 patients with treated LM, outcomes appear similar to patients with no history of LM.These data provide compelling evidence that the site of metastatic disease may be an important predictive biomarker for ICB treatment efficacy.These data are consistent with additional clinical reports of activity in non-liver metastatic disease with combinations of ICB and muti-tyrosine kinase inhibitors in a variety of cancers 45,46,52,53 .Recent data suggest that the liver has a immunosuppressive environment, which may confer specific resistance of LM to ICB 47,48 .Additional studies exploring the combination of BOT plus BAL with other agents, including standard-of-care chemotherapy, such as FOLFOX and bevacizumab (NCT05608044) in the first-line setting, may improve outcomes for patients with LM by treating patients in earlier lines of therapy with higher quality T effector cells and less tumoral heterogeneity.
In the context of a single-arm phase 1 study, outcomes with BOT plus BAL in a cohort of 101 response-evaluable (148 treated) patients with MSS mCRC are encouraging (Figs. 2 and 3).One limitation of this study is the lack of comparative efficacy against standard treatments for refractory MSS mCRC, such as trifluridine/tipiracil with or without bevacizumab, or regorafenib, in which response rates are known to be measurable in the low single digits [33][34][35] .However, most response-evaluable patients did not receive prior regorafenib (75%), trifluridine/tipiracil (86%) or both (69%), although most received prior bevacizumab (83%).Thus, the impact of prior treatments on efficacy and particularly survival remains to be elucidated.In addition, biomarker data on the study population, such as TMB, RAS, BRAF and PD-L1, were lacking in many patients.The role of PD-L1 expression in refractory MSS mCRC remains unclear but appears to have little predictive impact in first-generation ICB, and this appears to be the case with this combination, although conclusions cannot be made given the paucity of the data 54 .Another limitation of this study is that the efficacy data are still maturing, and, thus, the findings reported here may change and will be updated in a future publication.
Taken together, BOT was specifically designed to overcome the suppressive TME of immunologically 'cold' tumors by leveraging multiple mechanisms of action.BOT is distinct from prior drugs in the class based on its epitope binding and Fc functionality, which improve APC and NK cell binding, reduce complement fixation and enhance T reg depletion.BOT represents a new generation of ICB agents capable of eliciting meaningful clinical responses in challenging 'cold' tumor types that have historically not responded to ICB.Furthermore, these data underscore the importance of considering the site of metastatic disease as a potential predictive biomarker for ICB efficacy, specifically the liver, in the context of MSS mCRC.This finding highlights the need to stratify patients based on the presence or absence of LM in future immunotherapy trials and to explore novel strategies to overcome the immunosuppressive liver TME.A randomized phase 2 study of this combination is underway to confirm the comparative safety and efficacy of the BOT and BAL combination (NCT05608044).

Online content
Any methods, additional references, Nature Portfolio reporting summaries, source data, extended data, supplementary information, acknowledgements, peer review information; details of author contributions and competing interests; and statements of data and code availability are available at https://doi.org/10.1038/s41591-024-03083-7.).NLM was defined as patients with no history of LM (n = 17) or patients whose LM were resected or ablated without recurrence (treated; n = 2).Arrows indicate patients who, at the time of the data cutoff, were ongoing on treatment.a One patient later progressed.b One patient with a RECIST 1.1 response at 6 weeks had surgical resection of a target lesion that was considered clinical progression based on increase from nadir at 12 weeks after receiving steroids for an immune-mediated TRAE and was not confirmed; remaining target lesions then progressed.c Patient with treated LM (all other bars represent patients with no history of LM).NE, not evaluable.

Study design
The C-800-01 study is an open-label, phase 1, multicenter study that evaluates the safety, tolerability and pharmacokinetic and pharmacodynamic profiles of BOT with or without BAL and assesses the maximum tolerated dose in patients with advanced solid tumors.This study aims to determine the RP2D of BOT plus BAL (NCT03860272).Patients were enrolled at 14 sites across the United States.Patients with MSS mCRC were enrolled as part of the dose-escalation portion of the study (3 + 3 design) and later as a separate indication (expansion) cohort.BOT was given Q3W or Q6W, starting at dose level 0.1 mg kg −1 up to 3 mg kg −1 , administered IV for up to 2 years, or in combination with BAL 3 mg kg −1 Q2W administered IV for up to 2 years.A fixed-dose cohort evaluating BOT Q6W (150 mg) plus BAL Q3W (450 mg) administered IV for up to 2 years is also evaluated in this trial and is currently being evaluated in a phase 2 trial (BOT Q6W 75 mg versus 150 mg plus BAL Q2W 240 mg versus chemotherapy for refractory CRC; NCT0560844).Patients could be treated beyond progression.The C-800-01 study is currently still enrolling select indication cohorts, although the MSS mCRC expansion cohort was closed before the data cutoff.Since the original protocol (8 November 2018), there have been eight protocol amendments.The full protocol (Amendment 8) is provided as part of the Supplementary Information.A list of major changes in each amendment is summarized in Supplementary Table 9.Major changes included the addition of a safety monitoring committee (Amendment 5), the addition of a cohort to the Q6W combination arm to investigate fixed dosing (Amendment 5), an increase in the number of patients (multiple amendments) and an update of toxicity management guidelines (multiple amendments).

Study oversight
The

Statistical analysis
Data were evaluated as observed and are presented in a descriptive manner, with no imputation method for missing values unless otherwise specified.Descriptive statistics were used in general to summarize trial results, including means, medians, ranges and measures of variability.Qualitative variables were summarized by counts and percentages.The ORR per investigator assessment was evaluated over the entire trial period according to RECIST 1.1.For a best overall response of CR or PR, confirmation of the response was required.For patients with CR or PR, DOR was summarized using Kaplan-Meier methods, as was PFS and OS, for all patients.Median time to event(s) and 95% CI for the median were provided as required.
Exposure to BOT with or without BAL was characterized by duration (weeks), number of administrations, cumulative dose (mg kg −1 ), dose intensity (mg per kg per week), relative dose intensity (actual dose given / planned dose × 100) and number of dose delays, as a measure of compliance.Safety endpoints were tabulated by dose level, using descriptive statistics.Safety assessments were based on review of the incidence of adverse events (AEs); adverse drug reactions; immunogenicity; and changes in vital signs, electrocardiogram, body weight and laboratory values (hematology and serum chemistry).
AEs were coded according to the Medical Dictionary for Regulatory Activities (MedDRA).Severity of AEs was graded using NCI-CTCAE whenever possible.TEAEs are AEs with onset dates during the on-treatment period or the worsening of an event during the on-treatment period.Incidence of TEAEs, regardless of attribution, and TEAEs defined as related to BOT or BAL, were summarized by system organ class and preferred term and described in terms of severity and relationship to BOT or BAL.The on-treatment period was defined as time from first dose of study treatment to last dose of study treatment +30 d or the earliest date of new anti-cancer therapy −1 d, whichever occurred first.TRAEs (TEAEs related to BOT or BAL) were defined as those with onset dates or the worsening of an event during the extended on-treatment period, which was defined as time from the first dose of study treatment to last dose of study treatment +90 d or the earliest date of new anti-cancer therapy -1 d, whichever occurred first.Immune-mediated TRAEs were defined as immune-mediated TEAEs related to BOT or BAL that were treated with steroids or other immunosuppressants.All premature terminations were summarized by primary reason for study withdrawal.
The trial was conducted according to the protocol to enroll approximately 40 patients in expansion cohort 2. In an assigned dose level, patients in the dose-escalation and dose-expansion cohorts were treated in the same dose regimen and managed identically with assessments and procedures.In analyses, patients in the dose-escalation cohort are combined with the dose-expansion cohort at the same dose level, and we pooled escalation and expansion for efficacy and safety by dose.
Extended Data Fig. 3 | Gene expression analysis of pretreatment tumor tissue in patients with microsatellite stable metastatic colorectal cancer (n=38).The following plots compare patient outcomes (nine patients with partial responses [PRs], 18 with stable disease [SD] of at least 12 weeks, and 11 with progressive disease [PD]) across published gene signatures.Bulk RNA-Seq expression data was derived from pretreatment samples and the log2 gene transcripts per million (TPM) counts data were transformed to z-score values.The gene signatures were then calculated by averaging the gene expression values sample-wise and the results were compared across outcomes.Statistical comparisons used a two-sided nonparametric Dunn test and adjusted p-values were calculated with the Bonferroni method.(a) The interferon gamma (IFNy) signature (Ayers et al. 31 ) has been used to evaluate immune checkpoint blockade therapies for treating various cancer types.The upregulation of genes in the IFNy signature are indicative of a robust immune response to cancer.(b) The neutrophil signature (Bagaev et al. 32 ) includes a set of genes that are expressed by neutrophil cells in response to inflammation and infection.Upregulation of this signature can be used as an indicator of a poor response to checkpoint inhibitors.(c) The other signatures from Bagaev et al. 32 provide additional biomarkers for probing the immune status of patients with cancer, predicting therapeutic responses, and guiding individual immunotherapy approaches.CAF, cancer-associated fibroblast; DC, dendritic cell; EMT, epithelial-to-mesenchymal transition; MHC, major histocompatibility complex; NK, natural killer; TAM, tumor-associated macrophage; T reg , regulatory T cells.

Extended Data Table 1 | Baseline demographics and disease characteristics in all dose-escalation cohorts (n = 83)
a One patient received prior CTLA-4 therapy in addition to prior PD-(L)1 therapy.

Extended Data Table 2 | Clinical efficacy and outcomes summary in all dose-escalation cohorts (n = 83)
a ORR is defined as the proportion of patients with a best overall response of CR or PR by RECIST 1.1.b Best overall response is defined as the best response recorded over all on-study timepoint assessments recorded before the start of a new anti-cancer therapy.Confirmed responses required confirmation after at least 28 d.c DCR is defined as proportion of patients with CR, PR or SD for at least 6 weeks.d CBR is defined as the proportion of patients with CR, PR or SD for at least 24 weeks after first dose of study drug.NE, not evaluable.

Fig. 2 |
Fig. 2 | Clinical efficacy by liver involvement in response-evaluable patients with MSS mCRC (n = 101).Liver involvement was characterized as patients with active LM, treated LM that were resected or ablated without recurrence or no history of LM. a, Best overall response.b, Response over time.a Indicates a RECIST 1.1-confirmed CR or PR.The first blue bar on the right represents the CR. Articlehttps://doi.org/10.1038/s41591-024-03083-7 liver metastases Time from start of therapy (months)

Fig. 4 |
Fig. 4 | Responder characteristics (n = 19).NLM was defined as patients with no history of LM (n = 17) or patients whose LM were resected or ablated without recurrence (treated; n = 2).Arrows indicate patients who, at the time of the data cutoff, were ongoing on treatment.a One patient later progressed.b One patient with a RECIST 1.1 response at 6 weeks had surgical resection of a target lesion that

Clinical outcomes by liver involvement in response-evaluable patients with MSS mCRC
(n = 101).Liver involvement was characterized as patients with active LM, treated LM that were resected or ablated without recurrence or no history of LM.No active LM included patients with treated LM together with patients with no history of LM. a, PFS.b, OS.
://doi.org/10.1038/s41591-024-03083-745.Fakih, M. et al.Regorafenib, ipilimumab, and nivolumab for patients with microsatellite stable colorectal cancer and disease progression with prior chemotherapy: a phase 1 nonrandomized clinical trial.JAMA Oncol.9, 627-634 (2023).46.Fakih, M. et al.Regorafenib plus nivolumab in patients with mismatch repair-proficient/microsatellite stable metastatic colorectal cancer: a single-arm, open-label, multicentre phase 2 study.EClinicalMedicine 58, 101917 (2023).International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material.If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. https C-800-01 study was conducted in compliance with the Declaration of Helsinki and International Conference on Harmonization Guidelines for Good Clinical Practice and was approved by the institutional review EndpointsThe primary endpoint was to assess the occurrence of any DLTs in patients in the monotherapy and combination therapy dose-escalation cohorts during the first 28 d of treatment.Secondary endpoints